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Cdc Ii

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ICON
4-6 years
preferred by company
10 Jan. 30, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Coordinator II (CDC II)

Job Locations: India – Chennai | Bangalore | Trivandrum
Work Model: Office with Flex (Hybrid)
Employment Type: Full-Time
Experience Required: 4–6 Years
Job Requisition ID: JR141730
Industry: Clinical Research | Clinical Data Management | CRO

About ICON plc

ICON plc is a global leader in healthcare intelligence and clinical research, supporting the development of innovative therapies that improve patient outcomes worldwide. With a strong focus on quality, regulatory compliance, and data-driven clinical development, ICON partners with pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials.

Role Overview

The Clinical Data Coordinator II (CDC II) supports end-to-end clinical data management activities for global clinical studies. This role works closely with Clinical Data Scientists and Study Leads to ensure accurate, complete, and timely clinical trial data. The position requires hands-on experience in eCRF maintenance, data reconciliation, and issue resolution within regulated clinical research environments.

Key Responsibilities

  • Support the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and study-specific procedures

  • Perform reconciliation of clinical and third-party data in accordance with edit check specifications and data review plans

  • Track, analyze, and communicate study-level data metrics and task status to Clinical Data Scientists, project teams, and functional management

  • Address data-related queries and recommend effective solutions to data issues

  • Perform root cause analysis to identify and resolve recurring data discrepancies

  • Ensure compliance with internal SOPs, study protocols, and regulatory requirements

  • Collaborate with cross-functional teams to support high-quality data delivery

Required Qualifications

  • Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or a related discipline

  • 4–6 years of relevant experience in clinical data management within a CRO, pharmaceutical, or biotechnology organization

  • Working knowledge of clinical data management processes and lifecycle activities

  • Experience using clinical data management systems such as Medidata Rave, Oracle RDC, or equivalent platforms

  • Strong attention to detail with the ability to manage multiple priorities in a fast-paced environment

  • Effective written and verbal communication skills

  • Ability to collaborate across global and cross-functional teams

Preferred Skills

  • Knowledge of ICH-GCP guidelines and regulatory standards

  • Experience supporting Phase I–IV clinical trials

  • Familiarity with third-party data sources and reconciliation processes

Work Environment and Benefits

ICON offers a flexible hybrid work model supported by competitive compensation and comprehensive benefits. These include health insurance options, retirement planning, paid leave programs, employee wellness initiatives, and access to global employee assistance resources.

Diversity and Equal Opportunity

ICON is committed to fostering an inclusive and diverse workplace. All qualified applicants will receive equal consideration for employment without discrimination based on race, gender, disability, age, or any other protected status.